better Biotech Pharma Job in Massachusetts

resource to variouscorrectional facilitieswithin the State of Massachusetts...

Job Title Clinical Research Assistant II Requisition Number 09-2533 Organization BIDMC Research Division - Department 01055200 - General Medicine Job Category Research-RES City Boston State MA Grade 06 Status Full-Time Shift Day Job Description This a one-year full time position with the potential to extend up to 3 years. Reporting to the Program Manager, under the direction of the Principal Investigator, the incumbent is responsible for recruitment, screening and enrolling of patients for participation in

MAJOR RESPONSIBILITIES: Design and maintain databases for storage and retrieval of research data. Write computer programs to combine data from separate computer files to allow comparison of data from different sources. Instruct and supervise other personnel (data entry clerks, research assistants) in data management including merging and updating existing databases. Collaborate with program staff on the design and analysis of biostatistics aspects of research protocols. Create SAS/SPSS applications

various correctional facilities within the State of Massachusetts...

various correctional facilities within the State of Massachusetts...

Our client, a large medical device company in Raynham, is seeking an experienced Clinical Data Manager with strong Oracle Clinical experience to work with them to complete a large data management project. The Clinical Data Manager will: - Be responsible for overall database maintenance, data quality, and project management - Interact with clinical team on a daily basis to ensure overall quality and integrity of the data - Conduct Data Review and Validation procedures (data review; query integration) - Develop

The Clinical Data Manager with Cardiovascular experience, and EDC experience reviews data; assists in database design and testing; designs CRFs and guidelines; designs and tests logic checks; generates queries for missing or discrepant data; utilizes tools/systems to code medical terms and medications. Works with Clinical Monitoring, Medical Affairs, Database Development, Biometrics and Project Management personnel to resolve project related issues; provides input into the Dept. SOP s and process improvements

The new Clinical and Translational Investigation Program (CTIP) in the Division of Pediatric Hematology/Oncology, seeks applications for a Masters-level Biostatistician. This position will focus on maintenance and data mining analyses of an international database of neuroblastoma. Applicants must demonstrate high proficiency in statistical computing; SAS experience strongly preferred. Masters degree in biostatistics, statistics, or related field required. ~MN~

The new Clinical and Translational Investigation Program (CTIP) in the Division of Pediatric Hematology/Oncology seeks applications for a masters-level Biostatistician staff position. This position will focus on statistical analysis of pediatric cancer clinical and biological trials. Applicants must demonstrate high proficiency in statistical computing; SAS experience strongly preferred. Masters degree in biostatistics, statistics, or related field required. ~MN~

Licensed to practice in Massachusetts...

in the company s home state of Massachusetts...

Title Biostatistician I Department Medicine-Hematology/Oncology Job Posting Description The new Clinical and Translational Investigation Program (CTIP) in the Division of Pediatric Hematology/Oncology, seeks applications for a Masters-level Biostatistician. This position will focus on maintenance and data mining analyses of an international database of neuroblastoma. Applicants must demonstrate high proficiency in statistical computing; SAS experience strongly preferred. Masters degree in biostatistics, statistics

Title Biostatistician I Department Medicine-Hematology/Oncology Job Posting Description The new Clinical and Translational Investigation Program (CTIP) in the Division of Pediatric Hematology/Oncology seeks applications for a masters-level Biostatistician staff position. This position will focus on statistical analysis of pediatric cancer clinical and biological trials. Applicants must demonstrate high proficiency in statistical computing; SAS experience strongly preferred. Masters degree in biostatistics,

Job Title Clinical Research Assistant I Requisition Number 09-2476 Organization BIDMC Research Division - Department 01010040 - Med-Cardiovascular Spec Fund Job Category Research-RES City Boston State MA Grade 05 Status Full-Time Shift Day Position Details This requistion replaces 09-2347 Job Description Dynamic research assistant to work on epidemiologic studies evaluating the role of behavioral and environmental exposures on cardiovascular disease outcomes. Duties Study coordination Maintain study databases

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our Midwestern region. The clinical research

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our Midwestern region. The clinical research

Thoughtful Science. Tailored Solutions. NERI is a full-service Contract Research Organization that provides customized, global clinical trial solutions and registry services to pharmaceutical, biotechnology, biomaterial, and medical device companies. NERI also has notable experience collaborating on federally-funded research with organizations like the National Institutes of Health. Since its founding in 1986, NERI has earned widespread recognition for its scientific credibility, efficiency, and expertise

Registration as a Pharmacist in Massachusetts is required...

- Bachelor's degree is required - Licensure Required - Experience is required - Clinical Pharmacists at Tufts Medical Center work closely with other health practitioners to meet the various needs of our patients. The department's long-standing, effective relationship with physicians and nurses provides a friendly, collaborative and nurturing environment where pharmacists truly participate in making therapeutic decisions for every patient. Pharmacists review and approve medication orders, monitor drug therapies

Job Description: General Summary: This position is responsible for biostatistical activities in support of clinical trials including: generating data tables, patient data listings and reports using SAS; preparing statistical analysis plans; contributing to the statistical section of clinical trial protocols; reviewing analysis of clinical trial data. Duties and Responsibilities: Under direct supervision performs the following duties: - Generates statistical summary tables, patient data listings and reports

Our client is a major manufacturer of Class III medical devices. They are looking for a Sr. Clinical Research Associate who will conduct clinical studies in support of regulatory submissions as well as Marketing. The Sr.CRA will help prepare such clinical study documents as protocols, case reports and study summaries. The Sr. CRA will also coordinate physician contracts in order to assure that clinical projects and the required reports are completed in a timely manner. In addition, this individual will be responsible

We have an immediate need for an Assay Development Scientist in the Boston area. Participate in the advancement of our preclinical and clinical programs through the execution of assay development and sample analysis from animal and patient samples under GLP conditions. Identify issues with materials, processes, or equipment and work effectively with others to solve problems affecting the lab. Analyze and compile data, prepare and present technical reports. Strong organizational skills, the ability to

Pharmacist Location MA Taunton Department State of Massachusetts SOPS ID 962 of openings 1 Description...

Biostatistician Requisition ID 31332 Full/Part Time x Location Marlborough MA Description General Summary: This position is responsible for biostatistical activities in support of clinical trials including: generating data tables, patient data listings and reports using SAS; preparing statistical analysis plans; contributing to the statistical section of clinical trial protocols; reviewing analysis of clinical trial data. Duties and Responsibilities: Under direct supervision performs the following duties

Every day, Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. KSR is the first and largest scientific staffing company in the world, and we currently have an exciting Oracle Clinical Global Librarian position available in the Mansfield MA area. By working with Kelly Scientific Resources, you will receive: - Competitive pay - Eligibility to a comprehensive benefits package - Access to the Kelly Science Learning Center - The opportunity to gain experience

The person hired for this position will be responsible for processing serious adverse events in oncology clinical trials, focusing on the evaluation and reporting of cases in accordance with global safety regulations, departmental standard operating procedures and company policies. This individual will track cases from receipt to closure, perform verification of safety data and will utilize clinical/pharmacovigilance judgement in coding of serious events and synthesizing complex clinical information into accurate

Are you looking for a change? Do you want to succeed in a company that values quality of life for its employees? Then consider working at Harvard Clinical Research Institute, Inc. (HCRI). HCRI is an academic research organization that provides integrative solutions to support clinical trials and other clinical research. Working within the unique world-class patient care and research environment of the Harvard Medical School and affiliated institutions, we uphold the highest academic and ethical principles

Developed and operated by the University of Massachusetts Medical School Commonwealth Medicine is the school...s programs have been instrumental in assisting Massachusetts health care agencies and those in 19...

City Waltham State MA Job Title Clinical Research Associate Description SUMMARY OF POSITION: Participates in clinical research programs by assisting with the development of study protocols, case report forms, clinical reports, performing site monitoring visits, and interfacing with site coordinators, field clinical staff, and other company representatives. ESSENTIAL FUNCTIONS: . Ensure that documentation from investigators and investigational sites meets FDA/GCP/ICH requirements. . Assist in designing, planning

Senior Clinical Research Associate Job Type :Full Time Career Level :Experienced (Non-Manager) Education :Master's Degree Job Description : Position Description: A successful candidate, as a member of the Clinical Affairs group, will work collaboratively with multi-disciplinary teams to support the development of new assay test systems and laboratory services in the areas of prenatal, neonatal and child health. This role will initiate, coordinate, and take responsibility for developing supporting documents

Business Unit: NIBR Country: USA Company/Legal Entity: USA Novartis Institutes for BioMedical Research, Inc., Cambridge, MA Posting Functional Area: Development Employment Type: Permanent The Biomarker Data Analyst contributes to drug development efforts by providing high-quality and timely statistics and bioinformatics expertise in the areas of Biomarkers and Imaging (B&I) data analysis, integration and interpretation.Major ActivitiesProvide high added value to B&I components of drug projects

NIBR Country USA Work Location United States Massachusetts Company Legal Entity USA Novartis Institutes for...

The Senior Biostatistician fills a critical role within the Biometrics Department analyzing and interpreting confidential data from a variety of sources. Under minimal supervision the Senior Biostatistican is capable of working on highly complex projects suggesting analyses, compiling reports, charts and tables and interpreting results based on established statistical methods, relying on prior experience and judgment. Timeliness, excellent communication and professionalism are essential as staff in this position

Our client is an international Top 20 CRO that is rapidly growing. They have ambitious goals to be a Top 5 CRO within 5 years. But they need your help to get there. As one of the Sr Biostatisticians, you ll be working on projects with industry leading clients in a variety of therapeutic areas including oncology, cardiology, and even medical devices. With a proven 20+ year history of successful FDA submissions on behalf of clients and cultivating a culture of internal advancement, this is a great opportunity

Generous benefits package offered at 20 hours per week a variety of insurance coverages offered at 24 hours per week; 3 weeks of vacation to start. South Shore Medical Center (SSMC) is an independently owned, multi-specialty private practice of over 40 physicians engaged in internal medicine, pediatrics, surgery, family medicine and obstetrics/gynecology. Since 1962, SSMC has provided primary medical care as well as a variety of specialty and ancillary services to patients throughout the South Shore

A growing pharmaceutical company in the Boston area has 4 open NDA's and needs a qualified professional to build a department from the ground up with the focus on bringing all the trials in-house. In addition to their own products, the company is working on several products with major pharmaceutical partners. The company has excellent funding and promising projects point to a bright future. This is a unique opportunity to dramatically impact the future of a pharmaceutical company. You will be able to creatively

Kforce Clinical Research is always looking to build new relationships with experienced Regional Clinical Research Associates for future opportunities. If you are qualified and interested in hearing about potential opportunities when they become available, please apply today! At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's

Description Clinical Data Manager works collaboratively with Clinical Operations, Biometrics, PVG, Regulatory and other staff to meet project deliverables. The successful candidate will also have the ability to gather, organize, and analyze clinical data from multiple data sources. The incumbent will provide oversight to CROs, while performing extensive hands-on Clinical Data Management activities from protocol design through regulatory submission. This position will offer the ability to work in a stable

RESPONSIBILITIES: The main responsibility of this position is to manage the data management tasks requested by clients. Candidate must be able to take a clinical trial from beginning to end. Develop data management plans including required supporting documentation. Manage development of the specification documents for database tables, data entry screens, data derivations and edit check programming. Complete/manage testing of database and edit checks. Review data, produce queries and review

Established mid sized CRO has an immediate need for a Director of Biometrics. Details are as follows: The Director of Biometrics will manage a growing department providing vision, leadership and mentoring for personnel in the groups. This highly visible position has responsibility for successful coordination and execution of projects involving biostatistics and SAS Programming functional areas, interaction with clients, facilitation of effective inter-and intra-departmental relationships, oversight of

Clinical Research Coordinator Job ID: 19210 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary This position will work within the Division of Women's Cancers: Breast Oncology Center and supports the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The Clinical Research Coordinator performs basic technical procedures as directed. Collects medical data from paper and electronic

Clinical Research Coordinator Job ID: 19191 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary Eligibility screening, recruiting and enrolling patient and clinician participants in primarily sociobehavioral research studies; collecting data from study participants through paper questionnaires, structured qualitative interviews, computerized self-administered questionnaires, and audio recording devices; using electronic databases to track accrual and data

Clinical Research Coordinator III Job ID: 19176 Date Closed: 11/02/2009 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary Coordinates study enrollment, protocols treatment, and follow-up care for patients participating in clinical trials by working as a team with principal investigators, nursing, clinicians, both internal and external clinical trial regulatory groups (DFCI-OHRS, QACT) and other involved staff. Manages treatment protocol submissions (amendments

Clinical Research Coordinator III Job ID: 19175 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary Coordinates study enrollment, protocol treatment, and follow up care for patients participating in clinical trials by working as a team with principal investigators, nursing, clinicians, both internal and external clinical trial regulatory groups (DFCI-OHRS). Manages protocol submissions (amendments, continuing reviews, study audits) in a timely manner. Schedules

trials at the Dana Farber Cancer Institute Massachusetts General Hospital and many other clinics and...

Clinical Research Manager - Pediatric Oncology Job ID: 18143 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary The Clinical Research Manager (CRM) in collaboration with the programs physicians and research nursing staff is responsible for the design, implementation and evaluation of their programs clinical research activities, related regulatory oversight, and direct supervision of their program's clinical research staff. The CRM operationally reports

Clinical Research Coordinator IV Job ID: 18941 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary Coordinates study enrollment, protocols treatment, and follow-up care for patients participating in clinical trials by working as a team with principal investigators, nursing, clinicians, both internal and external clinical trial regulatory groups (DFCI-OPRS, QACT) and other involved staff. Manages treatment protocol submissions (amendments, continuing reviews

Clinical Research Coordinator II - Pediatric Oncology Job ID: 18637 Location: Full/Part Time: Full-Time Regular/Temporary: Regular Return to Previous Page Job Summary This position is for a Clinical Research Coordinator II to work full-time on a psychosocial project involving interviews and assessment of 18-24 year old daughters of women who are positive for a cancer predisposition gene. The person hired will have a wide range of tasks for this 3-year project including subject ascertainment, IRB contact

Our Client is a growing Biotech with strong funding and is focused on solving the truly challenging problems of unique diseases. They are committed to new innovative technology, and methods that focus on targeting the root cause of various diseases. In this position you will be need to provide support and leadership on project and protocol teams. You will be in charge of managing external statisticians and SAS programmers who support these teams. Also you will participate in the protocol development process

active memberships in the Drug Information Association Massachusetts Biotechnology Council Society for Clinical Data Management...